Over-expression of Hsp27 does not influence disease in the mutant S0D1G93A mouse model of amyotrophic lateral sclerosis

• Published in: Journal of neurochemistry Vol. 106; no. 5; pp. 2170 - 2183
• Main Authors: KRISHNAN, Jyothsna, VANNUVEL, Kayleen, ANDRIES, Maria, WAELKENS, Etienne, ROBBERECHT, Wim, VAN DEN BOSCH, Ludo
• Format: Journal Article
• Language: English
• Published: Oxford Blackwell 2008
• Subjects: Biological and medical sciences; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Diseases of striated muscles. Neuromuscular diseases; Medical sciences; Neurology; Animal model; Cardiovascular disease; Superoxide dismutase; HSPB1; Motor neuron; Vascular disease; Aggregation; Heat shock protein; Degenerative disease; chaperones; Human; Nervous system diseases; Enzyme; Amyotrophy; Acute; Chaperone; Rodentia; Amyotrophic lateral sclerosis; Spinal cord ischemia; Striated muscle disease; Vertebrata; Chronic; small heat shock proteins; Mammalia; Mouse; protein aggregation; Central nervous system disease; Oxidoreductases; Spinal cord disease
• ISSN: 0022-3042; 1471-4159